Canonical Allele Identifier: CA2658964612
Gene: MSH6 HGNC NCBI

Linked Data

gnomAD v4: 2-47782979-GCCAGCGTGCCAGCCCCGCCCCTACCCA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47782984_47783010del , CM000664.2:g.47782984_47783010del GRCh38
NC_000002.11:g.48010123_48010149del , CM000664.1:g.48010123_48010149del GRCh37
NC_000002.10:g.47863627_47863653del NCBI36
NG_007111.1:g.4838_4864del , LRG_219:g.4838_4864del

Transcript Alleles

HGVS Amino-acid Change
ENST00000652107.1:c.-37-7943_-37-7917del ENSP00000498629.1:n.-37-7943_-37-7917del
ENST00000606499.1:c.-37-7943_-37-7917del ENSP00000475605.1:n.-37-7943_-37-7917del
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